Reinhardt A, Cadden S, Sands J A
J Virol. 1978 Feb;25(2):479-85. doi: 10.1128/JVI.25.2.479-485.1978.
Various unsaturated fatty acids (notably palmitoleic acid and oleic acid) interfered with plaque production by the lipid-containing bacteriophage PR4 on lawns of Escherichia coli. Addition of fatty acid to give 50 mug/ml ( approximately 0.2 mM) at the time of infection prevented phage replication. If, however, the fatty acid was added after infection, normal amounts of phage were produced. If the fatty acid was added (to 50 mug/ml) to the host cell culture a long enough time before infection such that the fatty acid concentration in the growth medium at the time of infection was reduced to less, similar5 mug/ml (due to fatty acid incorporation by the host cells), normal phage replication occurred also. Neither palmitoleic acid nor oleic acid prevented PR4 attachment to E. coli. Several types of experiments indicated that it is the entry process of the virus that is inhibited by these fatty acids. Specifically, if the fatty acid was added at the time of infection, the host cells were not killed by the virus and no detectable amounts of viral protein were synthesized. In addition, experiments using purified radioisotope-labeled virions showed directly that entry is inhibited. Mutants of PR4 that did replicate in the presence of oleic acid arose spontaneously at a frequency of 10(-6). Three of these mutants that have been further characterized have protein and phospholipid compositions indistinguishable from those of wild-type PR4.
多种不饱和脂肪酸(尤其是棕榈油酸和油酸)会干扰含脂质噬菌体PR4在大肠杆菌菌苔上产生噬菌斑。在感染时添加脂肪酸使其浓度达到50微克/毫升(约0.2毫摩尔)可阻止噬菌体复制。然而,如果在感染后添加脂肪酸,则会产生正常数量的噬菌体。如果在感染前足够长的时间向宿主细胞培养物中添加脂肪酸(至50微克/毫升),使得感染时生长培养基中的脂肪酸浓度降至更低,类似5微克/毫升(由于宿主细胞摄取了脂肪酸),也会发生正常的噬菌体复制。棕榈油酸和油酸均不能阻止PR4附着于大肠杆菌。多种类型的实验表明,这些脂肪酸抑制的是病毒的进入过程。具体而言,如果在感染时添加脂肪酸,宿主细胞不会被病毒杀死,也不会合成可检测到的病毒蛋白。此外,使用纯化的放射性同位素标记病毒粒子进行的实验直接表明进入受到了抑制。能在油酸存在下复制的PR4突变体自发出现的频率为10^(-6)。其中三个经过进一步鉴定的突变体的蛋白质和磷脂组成与野生型PR4无异。